Bimetallic Ni-Fe total-methanation catalyst for the production of substitute natural gas under high pressure

被引:112
|
作者
Tian, Dayong [1 ]
Liu, Zhihong [1 ]
Li, Dandan [2 ]
Shi, Huiliang [1 ]
Pan, Weixiong [1 ]
Cheng, Yi [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Beijing Key Lab Green Chem React Engn & Technol, Beijing 100084, Peoples R China
[2] Beijing Univ Chem Technol, Sch Chem Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Bimetallic Ni-Fe; Catalyst; Total-methanation; High pressure; Substitute natural gas (SNG); CO CHEMISORPTION PROPERTIES; REDUCTION;
D O I
10.1016/j.fuel.2012.08.033
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The bimetallic Ni-Fe catalysts used in CO total-methanation reaction were prepared by the impregnation method on gamma-Al2O3 support for the production of substitute natural gas (SNG). The catalysts were characterized by N-2 physisorption measurements, field-emission scanning electron microscopy (FE-SEM), and H-2 temperature-programmed reduction (H-2-TPR). The methanation performance under the industrial total-methanation conditions (0.1-3.0 MPa, H-2/CO = 3.0-3.1) was studied in detail using Ni-Fe/gamma-Al2O3 as a heterogeneous catalyst. The results showed that the addition of Fe to the catalyst can effectively improve the catalytic activity of Ni/gamma-Al2O3, while the high activity of bimetallic Ni-Fe catalyst was attributed to the quality of Ni-Fe alloy in the catalyst in terms of the experimental results of H-2-TPR. The sample with appropriate Ni/Fe molar ratio of about 3 exhibited the highest CO conversion (near 100% at 225-550 degrees C) and the highest CH4 selectivity (over 99% at 300-450 degrees C) under the reaction pressure of 3.0 MPa. Furthermore, based on the systematic study of catalyst components, MgO in the catalyst can increase the reduction temperature of nickel oxide on the support. The silicon species as an impurity in the support play a negative role in the catalytic activity, especially for the CH4 selectivity. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:224 / 229
页数:6
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